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"AEGIST" Radiation Protection Device (Non-Sterile) - Taiwan Registration 3131ab1d92310b0ee0aed2286e4f805d

Access comprehensive regulatory information for "AEGIST" Radiation Protection Device (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3131ab1d92310b0ee0aed2286e4f805d and manufactured by JI SHENG MEDICAL COMPANY LIMITED. The authorized representative in Taiwan is JI SHENG MEDICAL COMPANY LIMITED.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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3131ab1d92310b0ee0aed2286e4f805d
Registration Details
Taiwan FDA Registration: 3131ab1d92310b0ee0aed2286e4f805d
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Device Details

"AEGIST" Radiation Protection Device (Non-Sterile)
TW: ่‰พๅ‰ๆ–ฏ็›พ ่ผปๅฐ„้˜ฒ่ญท็”จๅ…ท (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

3131ab1d92310b0ee0aed2286e4f805d

Ministry of Health Medical Device Manufacturing No. 007486

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Personal Protective Shield (P.6500)".

P Devices for radiology

P6500 Personal Shield

Produced in Taiwan, China

Dates and Status

Oct 19, 2018

Oct 19, 2023